Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Neoplasms and PCM1[original query] |
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| Targeted resequencing of the microRNAome and 3'UTRome reveals functional germline DNA variants with altered prevalence in epithelial ovarian cancer. Oncogene 2015 Apr 34 (16): 2125-37. Chen X, Paranjape T, Stahlhut C, McVeigh T, Keane F, Nallur S, Miller N, Kerin M, Deng Y, Yao X, Zhao H, Weidhaas J B, Slack F |
| The utilization of next-generation sequencing to detect somatic mutations and predict clinical prognosis of Chinese non-small cell lung cancer patients. OncoTargets and therapy 2018 11 2637-2646. Cao Liming, Long Long, Li Min, Yang Huaping, Deng Pengbo, Mao Xinru, Xiang Jianxing, Li Bing, Zhang Tengfei, Hu Chengpi |
| Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric reports 2021 1 13 (1): 45-56. Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer |
| MET gene alterations predict poor survival following chemotherapy in patients with advanced cancer. Pathology oncology research : POR 2022 12 28 1610697. Ko Jihoon, Jung Jaeyun, Kim Seung Tae, Hong Jung Yong, Park Sehhoon, Park Joon Oh, Park Young Suk, Lim Ho Yeong, Ahn Soomin, Kim Kyoung-Mee, Kang Won Ki, Lee Jeey |
| Genome-wide somatic mutation analysis of sinonasal adenocarcinoma with and without wood dust exposure. Genes and environment : the official journal of the Japanese Environmental Mutagen Society 2024 5 46 (1): 12. Lauri J Sipilä, Riku Katainen, Mervi Aavikko, Janne Ravantti, Iikki Donner, Rainer Lehtonen, Ilmo Leivo, Henrik Wolff, Reetta Holmila, Kirsti Husgafvel-Pursiainen, Lauri A Aalton |
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